A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915406



Internal ID22690624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31990511..31995701hg38UCSC Ensembl
chr11:32012057..32017247hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385191
hg195191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915406
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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